. Fe, 61.82.Pv, 64.70.Dv, 64.70.Pf The increase of positronium (Ps) formation in polymers (polyethylene and PMMA) cooled below the freezing temperature of molecular motions has been widely accepted to be due to positron interaction with weakly bound (trapped) electrons. For the first time, we will present results on a more complicated effect for monomers: in frozen hexanol below 100 K increase of ortho-Ps intensity (I 3 ) with elapsed time of the experiment could be inhibited by bleaching and therefore had the traditional explanation. However, around 200 K the increase of I 3 with elapsed time was not affected by light and had different nature, namely, reducing of inhibition effect due to formation of hydrogen bonds typical for the solid state structure. Many authors reported that the intensity of ortho-Ps (o-Ps), I 3 , increased during positron annihilation lifetime spectroscopy (PALS) measurements in polyethylene (PE) [9] and polymethyl-methacrylate (PMMA) [10] below the freezing temperature of the polymer structures. The increase was explained by trapped electrons captured in the shallow potential created among polymer structures below the freezing temperature of the molecular motions [10]. The trapped electrons are weakly bounded in a shallow potential and can be easily ejected by visible light with energy of 1 to 2 eV, which results in decrease of I 3 . Mentioned above enhancement of I 3 , as well as its bleaching by visible light, was also observed in monomer (solid cyclohexane) cooled at 77 K [2]. In this work, temperature dependence of annihilation characteristics in hexanol (CH 3 (CH 2 ) 4 CH 2 OH, melting temperature 221 K) was measured in the range